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Clinical Trial Summary

A multi-center, prospective, consecutive enrolled, observational registry. The population being studied includes all patients undergoing treatment of "de novo" lesions in native coronary vessels, saphenous vein graft and/or arterial bypass conduits with the COBRA PzF coronary stent system. The registry will primarily assess the rate of MACE (cardiac death, myocardial infarction and clinically driven target lesion revascularization.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03103620
Study type Observational
Source CeloNova BioSciences, Inc.
Contact
Status Completed
Phase
Start date September 10, 2015
Completion date December 31, 2017

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